Data / Medical devices / Resin, Root Canal Filling / Germany
FDA-registered makers of Resin, Root Canal Filling in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Resin, Root Canal Filling (product code KIF). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Resin, Root Canal Filling
- Product code
- KIF
- Country
- Germany
Makers of Resin, Root Canal Filling in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Gebr. Brasseler GMBH & Co. KG | LEMGO North Rhine-Westphalia, Germany | Exporter to the US, Specification developer | 3 | January 11, 2019 | 0 | 0 | 0 | api.fda.gov |
| Coltene/Whaledent GMBH & Co. KG | LANGENAU Baden-Wurttemberg, Germany | Exporter to the US, Manufacturer | 2 | January 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| DENTSPLY DETREY GmbH | KONSTANZ Baden-Wurttemberg, Germany | Manufacturer | 2 | February 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| S & C Polymer GMBH | ELMSHORN Schleswig-Holstein, Germany | Contract manufacturer, Manufacturer | 2 | July 24, 2013 | 0 | 0 | 0 | api.fda.gov |
| Voco GMBH | CUXHAVEN Lower Saxony, Germany | Manufacturer | 1 | July 3, 2025 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.